Canonical Allele Identifier: CA2576304890
Gene: TBX21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733374G>A , CM000679.2:g.47733374G>A GRCh38
NC_000017.10:g.45810740G>A , CM000679.1:g.45810740G>A GRCh37
NC_000017.9:g.43165739G>A NCBI36
NG_012166.1:g.5131G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.-81G>A MANE Select ENSP00000177694.1:n.-81G>A
ENST00000177694.1:c.-81G>A ENSP00000177694.1:n.-81G>A
NM_013351.1:c.-81G>A NP_037483.1:n.-81G>A
XM_011524698.1:c.-81G>A XP_011523000.1:n.-81G>A
NM_013351.2:c.-81G>A MANE Select NP_037483.1:n.-81G>A